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Foaming instant hand sanitizer - Medication Information

Product NDC Code 71303-207
Drug Name

Foaming instant hand sanitizer

Type Brand
Active Ingredients
Benzalkonium chloride .013 mg/ml
Route TOPICAL
Dosage Form LIQUID
Application Number part333E
Labeler Name RJ Schinner
Packages
Package NDC Code Description
71303-207-31 1000 ml in 1 bottle (71303-207-31)
71303-207-41 1000 ml in 1 bottle (71303-207-41)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
OTC Active Ingredient Section Active Ingredient: Benzalkonium Chloride 0.13% w/w

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Dosage and Administration Section Directions: Apply a small amount to palm. Briskly rub, covering hands with product until dry.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredient Section Inactive Ingredients: Water, Propylene Glycol, Cocamidopropyl Betaine, Aloe Barbadensis Leaf Juice, Tocopheral Acetate, Peg-& Glyceral Cocoate, Fragrance, Phenoxyethanol, Tetrasodium EDTA

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Indications and Usage Section Hand Sanitizer to help reduce bacteria on the skin that could cause disease. Intended for repeated use.

Purpose

Information about the drug product’s indications for use.
OTC Purpose Section Purpose: Antibacterial Agent

Spl product data elements

Usually a list of ingredients in a drug product.
Foaming Instant Hand Sanitizer 0.13% Benzakonium Chloride BENZALKONIUM CHLORIDE BENZALKONIUM .ALPHA.-TOCOPHEROL ACETATE PROPYLENE GLYCOL 1,2-DISTEARATE EDETATE SODIUM EDETIC ACID COCAMIDOPROPYL BETAINE PHENOXYETHANOL PEG-7 GLYCERYL COCOATE ALOE VERA LEAF

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Primary Display Label Primary Display Label

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep Out Of Reach Of Children Section Keep Out Of Reach Of Children: If swallowed, contact a physician or poison control center.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings Section Warnings: For External Use Only Contact with Eyes: If contact occurs, flush with water Stop Use if, in rare instances, redness or irritation develop. If condition persists more than 72 hours, contact a physician.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API